Publications by authors named "Azma Parhin"

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Full-length Isoform Sequencing for Resolving the Molecular Basis of Charcot-Marie-Tooth 2A.
Andrew B Stergachis, Elizabeth E Blue, Madelyn A Gillentine, Lee-Kai Wang, Ulrike Schwarze, Azma Parhin

Neurol Genet· October 2023

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Dominant-negative variant in SLC1A4 causes an autosomal dominant epilepsy syndrome.
Jonai Pujol-Giménez, Ghayda Mirzaa, Elizabeth E Blue, Giuseppe Albano, Danny E Miller, Azma Parhin

Ann Clin Transl Neurol· June 2023

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Full-length isoform sequencing for resolving the molecular basis of Charcot-Marie-Tooth 2A.
Andrew B Stergachis, Elizabeth E Blue, Madelyn A Gillentine, Lee-Kai Wang, Ulrike Schwarze, Azma Parhin

bioRxiv· February 2023

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New-onset Parkinsonism as a Covid-19 infection sequela: A systematic review and meta-analysis.
Syed Sami Ali, Afshan Mumtaz, Mohammad Aadil Qamar, Sameer Saleem Tebha, Azma Parhin

Ann Med Surg (Lond)· August 2022

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